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The Journal of Clinical Investigation|November 3, 2011
Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1Kevin Garofalo, Anke Penno, Brian P Schmidt, et al.
Journal of Biomolecular Screening|August 25, 2006
Two approaches to drug discovery in SOD1-mediated ALSWendy J Broom, Kristen E Auwarter, Jake Ni, et al.
Brain Pathology (Zurich, Switzerland)|June 29, 2010
Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusionsEric J Huang, Jiasheng Zhang, Felix Geser, et al.
Journal of Neurochemistry|November 8, 2005
Tetanus toxin fragment C fusion facilitates protein delivery to CNS neurons from cerebrospinal fluid in miceSusanna C Benn, Ilknur Ay, Elena Bastia, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 25, 2008
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALSMiriam H Meisler, Carsten Russ, Kate T Montgomery, et al.
Neurobiology of Disease|July 7, 2012
Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALSPaloma González-Pérez, Yubing Lu, Ru-Ju Chian, et al.
Brain : a Journal of Neurology|August 1, 2023
Repeated mild traumatic brain injury triggers pathology in asymptomatic C9ORF72 transgenic miceAydan Kahriman, James Bouley, Idil Tuncali, et al.
Human Molecular Genetics|August 12, 2010
Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granulesDaryl A Bosco, Nathan Lemay, Hae Kyung Ko, et al.
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